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Besides validation method of analysis, a fundamental requirement to perform agood laboratory practice is that the analytical instruments (TLC-scanner, sampleapplication system, video system, automated multiple development), the software,and the glasswares that will be used should be validated and calibrated. The validationof the instrument can be divided into design qualification (DQ), installation qualification(IQ), operation qualification (OQ), and performance qualification (PQ). The user of the instrument is obliged to maintain all documents; these include documentationsof DQ, IQ, OQ, and PQ, SOP for instrument calibration, SOP for cleaning andmaintenance, user book, log book, operating instruction, and software/hardwarevalidation certificates (Hahn-Dienstrop 2000). The availability of authentic standardreference compounds or BRM is very essential.
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